Karen E. Wain

1.2k total citations
28 papers, 567 citations indexed

About

Karen E. Wain is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Karen E. Wain has authored 28 papers receiving a total of 567 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 6 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Karen E. Wain's work include Genomics and Rare Diseases (17 papers), Genomic variations and chromosomal abnormalities (13 papers) and BRCA gene mutations in cancer (11 papers). Karen E. Wain is often cited by papers focused on Genomics and Rare Diseases (17 papers), Genomic variations and chromosomal abnormalities (13 papers) and BRCA gene mutations in cancer (11 papers). Karen E. Wain collaborates with scholars based in United States, Canada and Australia. Karen E. Wain's co-authors include Christa Lese Martin, David H. Ledbetter, W. Andrew Faucett, Erin Rooney Riggs, Matthew T. Oetjens, David T. Miller, Scott M. Myers, Wendy R. Uhlmann, Noralane M. Lindor and Viren Patel and has published in prestigious journals such as JAMA, American Journal of Psychiatry and JAMA Psychiatry.

In The Last Decade

Karen E. Wain

27 papers receiving 558 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Karen E. Wain United States	14	378	123	120	64	56	28	567
Sawona Biswas United States	10	374 1.0×	88 0.7×	110 0.9×	44 0.7×	24 0.4×	13	513
Kandamurugu Manickam United States	15	551 1.5×	113 0.9×	280 2.3×	150 2.3×	34 0.6×	34	928
Amanda L. Bergner United States	14	227 0.6×	70 0.6×	101 0.8×	13 0.2×	63 1.1×	32	640
Christopher Chun Yu Mak Hong Kong	13	240 0.6×	61 0.5×	192 1.6×	40 0.6×	18 0.3×	30	466
Li‐Ping Tsai Taiwan	13	284 0.8×	91 0.7×	160 1.3×	64 1.0×	21 0.4×	45	583
Melissa Martyn Australia	14	415 1.1×	89 0.7×	111 0.9×	58 0.9×	9 0.2×	40	647
Margaret Barrow United Kingdom	13	341 0.9×	231 1.9×	263 2.2×	25 0.4×	14 0.3×	18	738
Karen Bindels‐de Heus Netherlands	11	220 0.6×	99 0.8×	147 1.2×	37 0.6×	103 1.8×	23	570
Akella Radha Rama Devi India	15	147 0.4×	188 1.5×	176 1.5×	23 0.4×	18 0.3×	30	621
Ivan Macciocca Australia	16	319 0.8×	80 0.7×	211 1.8×	11 0.2×	15 0.3×	36	928

Countries citing papers authored by Karen E. Wain

Since Specialization

Citations

This map shows the geographic impact of Karen E. Wain's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Karen E. Wain with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karen E. Wain more than expected).

Fields of papers citing papers by Karen E. Wain

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Karen E. Wain. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Karen E. Wain. The network helps show where Karen E. Wain may publish in the future.

Co-authorship network of co-authors of Karen E. Wain

This figure shows the co-authorship network connecting the top 25 collaborators of Karen E. Wain. A scholar is included among the top collaborators of Karen E. Wain based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Karen E. Wain. Karen E. Wain is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Savatt, Juliann M., Melissa Kelly, Amy C. Sturm, et al.. (2025). Genomic Screening at a Single Health System. JAMA Network Open. 8(3). e250917–e250917. 5 indexed citations

Hallquist, Miranda L. G., Curtis R. Coughlin, Adam H. Buchanan, et al.. (2023). Defining critical educational components of informed consent for genetic testing: views of US-based genetic counselors and medical geneticists. European Journal of Human Genetics. 31(10). 1165–1174. 2 indexed citations

SoRelle, Jeffrey A., Birgit Funke, Jianling Ji, et al.. (2023). Slice Testing—Considerations from Ordering to Reporting. Journal of Molecular Diagnostics. 26(3). 159–167. 6 indexed citations

Simonovic, Nicolle, Jennifer M. Taber, Courtney L. Scherr, et al.. (2022). Uncertainty in healthcare and health decision making: Five methodological and conceptual research recommendations from an interdisciplinary team. Journal of Behavioral Medicine. 46(4). 541–555. 8 indexed citations

Shimelis, Hermela, Matthew T. Oetjens, Lauren K. Walsh, et al.. (2022). Prevalence and Penetrance of Rare Pathogenic Variants in Neurodevelopmental Psychiatric Genes in a Health Care System Population. American Journal of Psychiatry. 180(1). 65–72. 11 indexed citations

Ormond, Kelly E., Miranda L. G. Hallquist, Adam H. Buchanan, et al.. (2021). Defining the Critical Components of Informed Consent for Genetic Testing. Journal of Personalized Medicine. 11(12). 1304–1304. 18 indexed citations

Hallquist, Miranda L. G., Kelly E. Ormond, Juliann M. Savatt, et al.. (2021). Application of a framework to guide genetic testing communication across clinical indications. Genome Medicine. 13(1). 71–71. 18 indexed citations

Kelly, Melissa, Joseph B. Leader, Karen E. Wain, et al.. (2021). Leveraging population‐based exome screening to impact clinical care: The evolution of variant assessment in the Geisinger MyCode research project. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 187(1). 83–94. 25 indexed citations

Moreno-De-Luca, Andrés, Francisca Millan, Houda Zghal Elloumi, et al.. (2021). Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy. JAMA. 325(5). 467–467. 71 indexed citations

10.

Moreno-De-Luca, Andrés, Francisca Millan, Houda Zghal Elloumi, et al.. (2021). Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy. Obstetrical & Gynecological Survey. 76(7). 399–401.

11.

Wain, Karen E., Catherine Hajek, Juvianee Estrada‐Veras, et al.. (2020). Expanding the Phenotype of TUBB2A-Related Tubulinopathy: Three Cases of a Novel, Heterozygous TUBB2A Pathogenic Variant p.Gly98Arg. Molecular Syndromology. 12(1). 33–40. 8 indexed citations

12.

Wain, Karen E., Danielle R. Azzariti, Jennifer Goldstein, et al.. (2019). Variant interpretation is a component of clinical practice among genetic counselors in multiple specialties. Genetics in Medicine. 22(4). 785–792. 16 indexed citations

13.

Waggoner, Darrel, Karen E. Wain, Adrian M. Dubuc, et al.. (2018). Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 20(10). 1105–1113. 46 indexed citations

14.

Ormond, Kelly E., Miranda L. G. Hallquist, Adam H. Buchanan, et al.. (2018). Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background. Genetics in Medicine. 21(3). 727–735. 38 indexed citations

15.

Savatt, Juliann M., Danielle R. Azzariti, W. Andrew Faucett, et al.. (2018). ClinGen's GenomeConnect registry enables patient‐centered data sharing. Human Mutation. 39(11). 1668–1676. 24 indexed citations

16.

Wain, Karen E.. (2018). A Commentary on Opportunities for the Genetic Counseling Profession through Genomic Variant Interpretation: Reflections from an Ex‐Lab Rat. Journal of Genetic Counseling. 27(4). 747–750. 5 indexed citations

17.

Wain, Karen E., Marissa S. Ellingson, Jamie McDonald, et al.. (2014). Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart review. Genetics in Medicine. 16(8). 588–593. 54 indexed citations

18.

Riggs, Erin Rooney, Karen E. Wain, Melissa Savage, et al.. (2013). Towards a Universal Clinical Genomics Database: The 2012 International Standards for Cytogenomic Arrays Consortium Meeting. Human Mutation. 34(6). 915–919. 19 indexed citations

19.

Kotzer, Katrina E., et al.. (2013). Looking Back and Moving Forward: An Historical Perspective from Laboratory Genetic Counselors. Journal of Genetic Counseling. 23(3). 363–370. 22 indexed citations

20.

Wain, Karen E., et al.. (2012). Hereditary hemorrhagic telangiectasia and risks for adverse pregnancy outcomes. American Journal of Medical Genetics Part A. 158A(8). 2009–2014. 11 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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